Canonical Allele Identifier: CA2620715776

Gene: SART3

Linked Data

• gnomAD v4: 12-108530314-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108530314G>A , CM000674.2:g.108530314G>A	GRCh38
NC_000012.11:g.108924091G>A , CM000674.1:g.108924091G>A	GRCh37
NC_000012.10:g.107448221G>A	NCBI36
NG_012155.1:g.36075C>T
NG_012155.2:g.36076C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228284.8:c.1801-4C>T	ENSP00000228284.4:n.1801-4C>T
ENST00000546815.6:c.1747-4C>T MANE Select	ENSP00000449386.2:n.1747-4C>T
ENST00000651280.1:c.*903-4C>T	ENSP00000498612.1:n.*903-4C>T
ENST00000228284.7:c.1747-4C>T	ENSP00000228284.3:n.1747-4C>T
ENST00000431469.6:c.1639-4C>T	ENSP00000414453.2:n.1639-4C>T
ENST00000546728.5:c.*641-4C>T	ENSP00000449743.1:n.*641-4C>T
ENST00000546815.5:c.1801-4C>T	ENSP00000449386.1:n.1801-4C>T
ENST00000547528.5:c.*911-4C>T	ENSP00000446577.1:n.*911-4C>T
ENST00000548582.5:n.474-4C>T
ENST00000619503.4:n.683-4C>T
NM_014706.3:c.1747-4C>T	NP_055521.1:n.1747-4C>T
XM_005269241.3:c.1801-4C>T	XP_005269298.1:n.1801-4C>T
XM_011539026.1:c.883-4C>T	XP_011537328.1:n.883-4C>T
NM_014706.4:c.1747-4C>T MANE Select	NP_055521.1:n.1747-4C>T
XM_005269241.5:c.1801-4C>T	XP_005269298.1:n.1801-4C>T
XM_024449284.1:c.883-4C>T	XP_024305052.1:n.883-4C>T